Synthesis of new curcumin analogues from Claisen-Schmidt condensation

@article{Ziani2013SynthesisON,
  title={Synthesis of new curcumin analogues from Claisen-Schmidt condensation},
  author={N. Ziani and A. Sid and A. Demonceau and Quentin Willem and Benjamin Dassonneville and K. Lamara},
  journal={European Journal of Chemistry},
  year={2013},
  volume={4},
  pages={146-148}
}
A series of new curcumin analogues were obtained by Claisen-Schmidt condensation of substituted benzaldehydes with cyclohexanone derivatives using the ratio of 1:2 of ketone to aldehyde in dilute ethanolic solution under base catalyzed (NaOH) conditions at room temperature in good yields. The structures of the synthesized compounds were confirmed by data of IR, 1 H NMR, and 13 C NMR spectra. 
2 Citations

Figures from this paper

References

SHOWING 1-10 OF 21 REFERENCES
Chemistry of Heterocyclic Compounds
  • 577
Potential anticancer activity of turmeric (Curcuma longa).
  • 559
Biotransformation of curcumin through reduction and glucuronidation in mice.
  • M. Pan, T. M. Huang, J. Lin
  • Chemistry, Medicine
  • Drug metabolism and disposition: the biological fate of chemicals
  • 1999
  • 804
  • PDF
Pharmacokinetics and pharmacodynamics of curcumin.
  • 357
  • PDF
...
1
2
3
...